A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570576



Internal ID16357985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:96109020..96112697hg38UCSC Ensembl
Innerchr15:96652249..96655926hg19UCSC Ensembl
Innerchr15:94453253..94456930hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg383678
hg193678
hg183678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4743n54
Supporting Variantsnssv849070, nssv849068, nssv849069
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570576
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer